A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283881



Internal ID20493099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95761312..95761366hg38UCSC Ensembl
chr12:96155090..96155144hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736438
Supporting Variants
Samples
Known GenesNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283881
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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